The Linden Group Corp
United StatesFDA applicant, unverified
- Devices
- 2
What The Linden Group Corp makes
The Linden Group Corp manufactures medical display monitors, including the DIVA ZSP2105CMI with QUBYX PerfectLum bundle and the OptikView GUP2103CMI.
These Class II medical devices are based in the US and are listed in the FDA 510(k) regulatory registry.
Catalogue
DIVA ZSP2105CMI with QUBYX PerfectLum bundle Ref K160328
Regimes: 510(k) Registry: 510(k)OptikView GUP2103CMI Ref K191705
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does The Linden Group Corp have in the registry?
The registry currently lists 2 devices for The Linden Group Corp. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Linden Group Corp's devices?
Among its 2 most recently registered devices, The Linden Group Corp has devices listed in FDA 510(k) (2 devices).
What risk classes do The Linden Group Corp's devices fall under?
Among its 2 most recently registered devices, the classes recorded for The Linden Group Corp's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from The Linden Group Corp in the registry?
The most recently registered devices listed for The Linden Group Corp include DIVA ZSP2105CMI with QUBYX PerfectLum bundle and OptikView GUP2103CMI.